Device recall
Z-3290-2026: Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog…
FDA device recall · Class II · American Nitrile Operations Llc
Key facts
| Recall number (Z-number) | Z-3290-2026 |
|---|---|
| Recall event | 99748 |
| Product | Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number: 72-50900, 72-50901, 72-50902, 72-50903, 72-50904 Product Description: Blue Nitrile Patient examination gloves |
| Product code | LZA |
| Recalling firm | American Nitrile Operations Llc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220825 |
| FEI number | 3024755882 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database